18916-17-1 Usage
Description
Naringin dihydrochalcone, a member of flavonoids and a glycoside, is an artificial sweetener and flavonoid that has been isolated from various plants. It possesses antioxidant activity and is known for its intense sweetness and ability to scavenge ABTS, oxygen, and DPPH radicals in cell-free assays.
Uses
Used in Food Industry:
Naringin dihydrochalcone is used as an intense sweetener for its ability to provide sweetness to food products without adding significant calories. This makes it a suitable alternative for those looking to reduce their sugar intake or for individuals with diabetes.
Used in Pharmaceutical Industry:
Naringin dihydrochalcone is used as a strong antioxidant compound for its potential to protect cells from oxidative stress and damage. Its antioxidant properties make it a valuable ingredient in the development of pharmaceutical products aimed at promoting overall health and well-being.
Used in Allergy Treatment:
Naringin dihydrochalcone is used as an anti-allergic agent due to its ability to display anti-allergic activity. This application can be beneficial in the development of treatments for various allergic conditions and reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 18916-17-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,9,1 and 6 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 18916-17:
(7*1)+(6*8)+(5*9)+(4*1)+(3*6)+(2*1)+(1*7)=131
131 % 10 = 1
So 18916-17-1 is a valid CAS Registry Number.
InChI:InChI=1/C27H34O14/c1-11-20(33)22(35)24(37)26(38-11)41-25-23(36)21(34)18(10-28)40-27(25)39-14-8-16(31)19(17(32)9-14)15(30)7-4-12-2-5-13(29)6-3-12/h2-3,5-6,8-9,11,18,20-29,31-37H,4,7,10H2,1H3/t11-,18-,20-,21-,22+,23+,24+,25-,26-,27-/m0/s1
18916-17-1Relevant articles and documents
Synthetic method for naringin dihydrochalcone
-
Paragraph 0022, (2016/10/09)
The invention discloses a synthetic method for naringin dihydrochalcone. The method comprises the following steps that natural extract naringin is adopted as a raw material, alkali dissolution is performed and then filtering is performed; a polarity organic solvent is added, a catalyst is added, hydrogenation reduction is performed on the condition of the certain pressure, the catalyst is filtered away after hydrogen absorption is completed, the pH value is adjusted for crystallization, a product is obtained through filtration, and the naringin dihydrochalcone can be obtained; the liquid phase purity is 98.5% or above, and the molar yield is 96% or above.